C282Y and H63D Polymorphisms in Hemochromatosis Gene and Risk of Parkinson’s Disease

Author:

Duan Chunhong1,Wang Meiyun1,Zhang Yan2,Wei Xuxia1,Huang Yan1,Zhang Hongxia1,Cheng Lu1,Gai Zhongtao1

Affiliation:

1. Ji’nan Children’s Hospital, Ji’nan, Shandong, China

2. Ji’nan Center For Disease Control And Prevention, Ji’nan, Shandong, China

Abstract

Objective: A meta-analysis was performed to better clarify the association between hemochromatosis (HFE) gene and the risk of Parkinson’s disease (PD). Methods: Pooled odds ratio (OR) with 95% confidence interval (CI) was calculated from fixed- and random-effect models. Heterogeneity among studies was evaluated using the I2 and Q test. Egger’s test was used to estimate the publication bias. Results: We identified 8 articles with 9 independent studies for this meta-analysis. The present meta-analysis showed no significant association of Y allele with the risk of PD in dominant (OR = 0.87, 95% CI = 0.70-1.09), recessive (OR = 1.58, 95% CI = 0.61-4.10), and codominant (OR = 0.88, 95% CI = 0.72-1.09) models for C282Y. There were also no significant associations of D allele with the risk of PD in dominant (OR = 1.04, 95% CI = 0.87-1.24), recessive (OR = 1.23, 95% CI = 0.70-2.18), and codominant (OR = 1.04, 95% CI = 0.89-1.22) genetic models for H63D. No publication bias was detected. Conclusion: The meta-analysis indicated that C282Y and H63D polymorphisms in the HFE gene might not be associated with PD.

Publisher

SAGE Publications

Subject

Psychiatry and Mental health,Geriatrics and Gerontology,Clinical Psychology,General Neuroscience

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